A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204463



Internal ID20771503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7840382..7854019hg38UCSC Ensembl
chr1:7900442..7914079hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3813638
hg1913638
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318838
Supporting Variants
Samples
Known GenesPER3, UTS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204463
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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